Search Results - "Chiang, Ming Sum R"
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Preclinical pharmacology of glucosylceramide synthase inhibitor venglustat in a GBA-related synucleinopathy model
Published in Scientific reports (22-10-2021)“…Mutations in GBA , the gene encoding the lysosomal enzyme glucocerebrosidase (GCase), represent the greatest genetic risk factor for developing…”
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Exosome reporter mice reveal the involvement of exosomes in mediating neuron to astroglia communication in the CNS
Published in Nature communications (12-09-2019)“…Astroglia play active and diverse roles in modulating neuronal/synaptic functions in the CNS. How these astroglial functions are regulated, especially by…”
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Molecular and Functional Properties of Regional Astrocytes in the Adult Brain
Published in The Journal of neuroscience (06-09-2017)“…The molecular signature and functional properties of astroglial subtypes in the adult CNS remain largely undefined. By using translational ribosome affinity…”
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Differential Proliferation and Maturation of Subcortical Astrocytes During Postnatal Development
Published in Frontiers in neuroscience (08-05-2020)“…Astrocytes exhibit a region-dependent molecular and functional heterogeneity in the CNS. Although cortical astrocytes proliferate robustly during the first…”
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Molecular analysis of acute and chronic reactive astrocytes in the pilocarpine model of temporal lobe epilepsy
Published in Neurobiology of disease (01-07-2016)“…Abstract Astroglia, the most abundant glial cells in the mammalian central nervous system (CNS), are considered an emerging key player in seizure induction and…”
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Selective Deletion of Astroglial FMRP Dysregulates Glutamate Transporter GLT1 and Contributes to Fragile X Syndrome Phenotypes In Vivo
Published in The Journal of neuroscience (06-07-2016)“…How the loss of fragile X mental retardation protein (FMRP) in different brain cell types, especially in non-neuron glial cells, induces fragile X syndrome…”
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Astroglial FMRP modulates synaptic signaling and behavior phenotypes in FXS mouse model
Published in Glia (01-03-2021)“…Fragile X syndrome (FXS) is one of the most common inherited intellectual disability (ID) disorders, in which the loss of FMRP protein induces a range of…”
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